Prop. As prepared by Deville, metallic manganese has a reddish lustre, like bismuth; it is very hard and brittle; when powdered, it decomposes water, even at the lowest temperature. Dilute sulphuric acid dissolves it with great energy, evolving hydrogen. Sp. gr. 7·13. In an oxidised state manganese is abundant in the mineral kingdom, and traces of it have been found in the ashes of plants and in mineral waters.

The salts of manganese may be easily prepared in a state of purity by dissolving the precipitated carbonate in the acids. Most of them are soluble, and several are crystallisable.

Tests. Manganous salts are distinguished as follows:—The hydrates of potassium and sodium give white precipitates insoluble in excess, and rapidly turning brown. The presence of ammonium salts interferes with these tests. Ammonia gives similar results.

Ferrocyanide of potassium gives a white precipitate. Sulphuretted hydrogen gives no precipitate in acid solutions, and precipitates neutral solutions only imperfectly; but in alkaline solutions it gives a bright, flesh-coloured, insoluble precipitate, which becomes dark brown on exposure to the air. Sulphide of ammonium, in neutral solutions, also yields a similar precipitate, which is very characteristic. A compound of manganese fused with borax in the outer flame of the blowpipe gives a bead, which appears of a violet-red colour whilst hot, and upon cooling acquires an amethystine tint; this colour is lost by fusion in the inner flame. Heated upon platinum foil with a little carbonate of sodium, in the outer flame, it yields a green mass whilst hot, which becomes bluish green when cold.

Manganous Ace′tate. Mn(C2H3O2)2. Syn. Acetate of protoxide of manganese; Manganii acetas, L. Prep. 1. By neutralising concentrated acetic acid with manganous carbonate,

and evaporating the solution so that crystals may form.

Prop., &c. The crystals, when pure, are of a pale red colour; permanent in the air; soluble in alcohol, and 312 parts of water, and possess an astringent and metallic taste.—Dose, 5 to 10 gr., as an alterative, hæmatinic, &c.

Manganous Car′bonate. MnCO3. Syn. Carbonate of protoxide of manganese; Manganesii carbonas, L. Prep. Reduce the black oxide of manganese of commerce to fine powder, and after washing it in water acidulated with hydrochloric acid, dissolve it in strong hydrochloric acid, and evaporate the resulting solution to dryness; dissolve the residue in water, and add to the solution sufficient sodium carbonate to precipitate all the iron present; digest the mixed precipitate in the remainder of the liquid, filter, add ammonium sulphide until it begins to produce a flesh-coloured precipitate, then filter, and add sodium carbonate as long as a precipitate falls; lastly, well wash the newly-formed carbonate in water, and dry it by a gentle heat.

2. By directly precipitating a solution of the chloride with sodium carbonate, and washing and drying the powder as before.

Prop., &c. A pale buff or cream-coloured powder; insoluble in water; freely soluble in acids; exposed to a strong heat, it loses its carbonic acid, absorbs oxygen, and is converted into the red oxide. It is chiefly employed in the preparation of the other salts of manganese.